Canonical Allele Identifier: PA2825068251
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1432920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Glu14Asp
CA9043810
NM_000156.6:c.42G>C
CA402998384
NM_000156.6:c.42G>T